856591-70-3 Usage
Uses
Used in Pharmaceutical Research:
2-(2-furylmethylsulfanyl)pyridine is used as a ligand in coordination chemistry for its potential to form stable complexes with metal ions, which can be beneficial in the development of new pharmaceutical agents.
Used in Organic Synthesis:
As a building block, 2-(2-furylmethylsulfanyl)pyridine is utilized in the synthesis of various heterocyclic compounds, which are important in the creation of organic molecules with diverse applications.
Used in Antimicrobial Applications:
2-(2-furylmethylsulfanyl)pyridine is studied for its antimicrobial properties, making it a candidate for use in the development of new antibiotics or antimicrobial agents.
Used in Anticancer Research:
2-(2-furylmethylsulfanyl)pyridine is also being investigated for its potential anticancer properties, which could lead to its use in the development of novel cancer treatments.
Used in Chemical Compound Development:
Due to its unique structure and properties, 2-(2-furylmethylsulfanyl)pyridine serves as a valuable component in the development of new chemical compounds with specific applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 856591-70-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,6,5,9 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 856591-70:
(8*8)+(7*5)+(6*6)+(5*5)+(4*9)+(3*1)+(2*7)+(1*0)=213
213 % 10 = 3
So 856591-70-3 is a valid CAS Registry Number.
856591-70-3Relevant articles and documents
Versatile C(sp2)?C(sp3) Ligand Couplings of Sulfoxides for the Enantioselective Synthesis of Diarylalkanes
Dean, William M.,?iau?iulis, Mindaugas,Storr, Thomas E.,Lewis, William,Stockman, Robert A.
supporting information, p. 10013 - 10016 (2016/08/16)
The reaction of chiral (hetero)aryl benzyl sulfoxides with Grignard reagents affords enantiomerically pure diarylalkanes in up to 98 % yield and greater than 99.5 % enantiomeric excess. This ligand coupling reaction is tolerant to multiple substitution patterns and provides access to diverse areas of chemical space in three operationally simple steps from commercially available reagents. This strategy provides orthogonal access to electron-deficient heteroaromatic compounds, which are traditionally synthesized by transition metal catalyzed cross-couplings, and circumvents common issues associated with proto-demetalation and β-hydride elimination.
